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Reviews: (a) Guillier, F.; Orain, D.; Bradley, M. Chem. Rev. 2000, 100, 2091. (b) Dorwald, F. Z. Organic Synthesis on Solid Phase; Wiley-VCH: Weinheim, Germany, 2000. (c) Burgess, K. Solid-Phase Organic Synthesis; John Wiley & Sons: New York, 2000. (d) Handbook of Combinatorial Chemistry; Nicolaou, K. C., Hanko, R., Hartwig, W., Eds.; Wiley-VCH: Weinheim, Germany, 2002; Vols. 1 and 2.
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Selective S-alkylation of 4-mercaptophenol, see: Breitenbucher, J. G.; Johnson C. R.; Haight, M.; Phelan, J. C. Tetrahedron Lett. 1998, 39, 1295.
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0141490599
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European Patent 468531 A1, 1992
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Perfluoroalkylsulfanylphenol 2 has been used as a photoimaging compound, see: Wakamatsu, K.; Wakata, Y.; Satomura, M.; Namiki, T. European Patent 468531 A1, 1992.
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Wakamatsu, K.1
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Namiki, T.4
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23
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0141825235
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note
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Our recent study and an independent work from Lindsley (ref 10) demonstrated that amines could be retained on the SPE cartridge by adding acidic ion-exchange resin on top of the fluorous silica. No more acidic workup was needed prior to the SPE.
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24
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0037009729
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Lindsley, C. W.; Zhao, Z.; Leister, W. H.; Strauss K. A. Tetrahedron Lett. 2002, 43, 6319.
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Lindsley, C.W.1
Zhao, Z.2
Leister, W.H.3
Strauss, K.A.4
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25
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0141602129
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note
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2O (80/20). The first 8-mL fraction contained the desired product and the subsequent fraction eluted with MeOH contained the displaced fluorous tag.
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26
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0141713879
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note
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Purchased from Aldrich, loading 1.0-1.5 mmol/g, polystyrene with 1% cross linking with DVB. An average loading of 1.25 mmol/g was used for the calculation.
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